美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
71335-2558-1	71335-2558	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET	ORAL	20250123	N/A	ANDA	ANDA078245	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	25 mg/1; 100 mg/1	30 TABLET in 1 BOTTLE (71335-2558-1)
71335-2558-2	71335-2558	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET	ORAL	20250123	N/A	ANDA	ANDA078245	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	25 mg/1; 100 mg/1	90 TABLET in 1 BOTTLE (71335-2558-2)
71335-2558-3	71335-2558	HUMAN PRESCRIPTION DRUG	Losartan Potassium and Hydrochlorothiazide	Losartan Potassium and Hydrochlorothiazide	TABLET	ORAL	20250123	N/A	ANDA	ANDA078245	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM	25 mg/1; 100 mg/1	60 TABLET in 1 BOTTLE (71335-2558-3)